Canonical Allele Identifier: CA2805415476

Gene: IGF1R

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.98908936_98908937insCCCCCAAACACACCCAAC , CM000677.2:g.98908936_98908937insCCCCCAAACACACCCAAC	GRCh38
NC_000015.9:g.99452165_99452166insCCCCCAAACACACCCAAC , CM000677.1:g.99452165_99452166insCCCCCAAACACACCCAAC	GRCh37
NC_000015.8:g.97269688_97269689insCCCCCAAACACACCCAAC	NCBI36
NG_009492.1:g.264405_264406insCCCCCAAACACACCCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649865.1:c.1462+37_1462+38insCCCCCAAACACACCCAAC	ENSP00000496919.1:n.1462+37_1462+38insCCCCCAAACACACCCAAC
ENST00000650285.1:c.1462+37_1462+38insCCCCCAAACACACCCAAC MANE Select	ENSP00000497069.1:n.1462+37_1462+38insCCCCCAAACACACCCAAC
ENST00000268035.10:c.1462+37_1462+38insCCCCCAAACACACCCAAC	ENSP00000268035.6:n.1462+37_1462+38insCCCCCAAACACACCCAAC
ENST00000558762.5:c.1462+37_1462+38insCCCCCAAACACACCCAAC	ENSP00000453007.1:n.1462+37_1462+38insCCCCCAAACACACCCAAC
ENST00000558898.1:c.553+37_553+38insCCCCCAAACACACCCAAC	ENSP00000454115.1:n.553+37_553+38insCCCCCAAACACACCCAAC
ENST00000559582.1:n.369+37_369+38insCCCCCAAACACACCCAAC
ENST00000559925.5:n.1462+37_1462+38insCCCCCAAACACACCCAAC
NM_000875.4:c.1462+37_1462+38insCCCCCAAACACACCCAAC	NP_000866.1:n.1462+37_1462+38insCCCCCAAACACACCCAAC
NM_001291858.1:c.1462+37_1462+38insCCCCCAAACACACCCAAC	NP_001278787.1:n.1462+37_1462+38insCCCCCAAACACACCCAAC
XM_011521513.1:c.1525+37_1525+38insCCCCCAAACACACCCAAC	XP_011519815.1:n.1525+37_1525+38insCCCCCAAACACACCCAAC
XM_011521514.1:c.1525+37_1525+38insCCCCCAAACACACCCAAC	XP_011519816.1:n.1525+37_1525+38insCCCCCAAACACACCCAAC
XM_011521515.1:c.1525+37_1525+38insCCCCCAAACACACCCAAC	XP_011519817.1:n.1525+37_1525+38insCCCCCAAACACACCCAAC
XM_011521516.1:c.553+37_553+38insCCCCCAAACACACCCAAC	XP_011519818.1:n.553+37_553+38insCCCCCAAACACACCCAAC
XM_011521517.1:c.127+37_127+38insCCCCCAAACACACCCAAC	XP_011519819.1:n.127+37_127+38insCCCCCAAACACACCCAAC
XM_011521516.2:c.553+37_553+38insCCCCCAAACACACCCAAC	XP_011519818.1:n.553+37_553+38insCCCCCAAACACACCCAAC
XM_011521517.2:c.127+37_127+38insCCCCCAAACACACCCAAC	XP_011519819.1:n.127+37_127+38insCCCCCAAACACACCCAAC
XM_017022136.1:c.1537+37_1537+38insCCCCCAAACACACCCAAC	XP_016877625.1:n.1537+37_1537+38insCCCCCAAACACACCCAAC
XM_017022137.1:c.1537+37_1537+38insCCCCCAAACACACCCAAC	XP_016877626.1:n.1537+37_1537+38insCCCCCAAACACACCCAAC
XM_017022138.1:c.1537+37_1537+38insCCCCCAAACACACCCAAC	XP_016877627.1:n.1537+37_1537+38insCCCCCAAACACACCCAAC
XM_017022139.1:c.1099+37_1099+38insCCCCCAAACACACCCAAC	XP_016877628.1:n.1099+37_1099+38insCCCCCAAACACACCCAAC
XM_024449913.1:c.553+37_553+38insCCCCCAAACACACCCAAC	XP_024305681.1:n.553+37_553+38insCCCCCAAACACACCCAAC
NM_000875.5:c.1462+37_1462+38insCCCCCAAACACACCCAAC MANE Select	NP_000866.1:n.1462+37_1462+38insCCCCCAAACACACCCAAC
NM_001291858.2:c.1462+37_1462+38insCCCCCAAACACACCCAAC	NP_001278787.1:n.1462+37_1462+38insCCCCCAAACACACCCAAC